HuGE Literature Finder
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| H63D CG genotype of HFE is associated with increased risk of sporadic amyotrophic lateral sclerosis in a single population. Journal of integrative neuroscience 2020 10 19 (3): 495-499. Zhang Qing-Qing, Jiang Hong, Li Chun-Yan, Liu Ya-Ling, Tian Xin-Yi |
| Iron in Frontotemporal Lobar Degeneration: A New Subcortical Pathological Pathway? Neuro-degenerative diseases 2015 Nov . Gazzina Stefano, Premi Enrico, Zanella Isabella, Biasiotto Giorgio, Archetti Silvana, Cosseddu Maura, Scarpini Elio, Galimberti Daniela, Serpente Maria, Gasparotti Roberto, Padovani Alessandro, Borroni Barba |
| HFE p.H63D polymorphism does not influence ALS phenotype and survival. Neurobiology of aging 2015 Oct 36 (10): 2906.e7-2906.e11. Chiò Adriano, Mora Gabriele, Sabatelli Mario, Caponnetto Claudia, Lunetta Christian, Traynor Bryan J, Johnson Janel O, Nalls Mike A, Calvo Andrea, Moglia Cristina, Borghero Giuseppe, Monsurrò Maria Rosaria, La Bella Vincenzo, Volanti Paolo, Simone Isabella, Salvi Fabrizio, Logullo Francesco O, Nilo Riva, Giannini Fabio, Mandrioli Jessica, Tanel Raffaella, Murru Maria Rita, Mandich Paola, Zollino Marcella, Conforti Francesca L, Penco Silvana, , , Brunetti Maura, Barberis Marco, Restagno Gabriel |
| H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis. Neurobiology of aging 2013 May 34 (5): 1517.e5-7. van Rheenen Wouter, Diekstra Frank P, van Doormaal Perry T C, Seelen Meinie, Kenna Kevin, McLaughlin Russell, Shatunov Aleksey, Czell David, van Es Michael A, van Vught Paul W J, van Damme Philip, Smith Bradley N, Waibel Stefan, Schelhaas H Jurgen, van der Kooi Anneke J, de Visser Marianne, Weber Markus, Robberecht Wim, Hardiman Orla, Shaw Pamela J, Shaw Christopher E, Morrison Karen E, Al-Chalabi Ammar, Andersen Peter M, Ludolph Albert C, Veldink Jan H, van den Berg Leonard |
| Study of the HFE gene common polymorphisms in French patients with sporadic amyotrophic lateral sclerosis. Journal of the neurological sciences 2012 Jun 317 (1-2): 58-61. Praline Julien, Blasco Hélène, Vourc'h Patrick, Rat Valérian, Gendrot Chantal, Camu William, Andres Christian R, |
| H63D polymorphism in the hemochromatosis gene is associated with sporadic amyotrophic lateral sclerosis in China. European journal of neurology : the official journal of the European Federation of Neurological Societies 2011 Feb 18 (2): 359-61. He X, Lu X, Hu J, Xi J, Zhou D, Shang H, Liu L, Zhou H, Yan B, Yu L, Hu F, Liu Z, He L, Yao X, Xu |
| HFE gene mutations in a population of Italian Parkinson's disease patients. Parkinsonism & related disorders 2008 14 (5): 426-30. Biasiotto Giorgio, Goldwurm Stefano, Finazzi Dario, Tunesi Sara, Zecchinelli Anna, Sironi Francesca, Pezzoli Gianni, Arosio Pao |
| HFE H63D polymorphism is increased in patients with amyotrophic lateral sclerosis of Italian origin. Journal of neurology, neurosurgery, and psychiatry 2007 Mar 78 (3): 327. Restagno G, Lombardo F, Ghiglione P, Calvo A, Cocco E, Sbaiz L, Mutani R, Chiò |
| The association between H63D mutations in HFE and amyotrophic lateral sclerosis in a Dutch population. Archives of neurology 2007 Jan 64 (1): 63-7. Sutedja Nadia A, Sinke Richard J, Van Vught Paul W J, Van der Linden Michiel W, Wokke John H J, Van Duijn Cornelia M, Njajou Omer T, Van der Schouw Yvonne T, Veldink Jan H, Van den Berg Leonard |
| Increased incidence of the Hfe mutation in amyotrophic lateral sclerosis and related cellular consequences. Journal of the neurological sciences 2004 Dec 227 (1): 27-33. Wang Xin-Sheng, Lee Sang, Simmons Zachary, Boyer Philip, Scott Kevin, Liu Wenlei, Connor Jam |
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- Page last updated:Mar 22, 2023
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